Canonical Allele Identifier: CA2275548049
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516101C= , CM000679.2:g.75516101C= GRCh38
NC_000017.10:g.73512182C= , CM000679.1:g.73512182C= GRCh37
NC_000017.9:g.71023777C= NCBI36
NG_013041.1:g.4574C=
NG_033152.1:g.4483G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-368C= ENSP00000406559.4:n.-368C=
ENST00000679370.1:n.158C=
ENST00000434205.7:c.-368C= ENSP00000406559.3:n.-368C=
XM_006721821.2:c.-533C= XP_006721884.1:n.-533C=